Diastereoselectivity of the α,α-diphenylprolinol trimethylsilyl ether-catalyzed two-component domino reactions: Toward cyclohexanes with six stereogenic centers

Tetrahedron

Volumn 68, Issue 2, 2012, Pages 481-487

  Wong, Chiong Teck ^a  

^a INSTITUTE OF HIGH PERFORMANCE COMPUTING   (Singapore)

Author keywords

Ab initio methods; Cascade domino reaction; Density functional theory methods; Diastereoselectivity; Reaction mechanism

Indexed keywords

ALPHA,ALPHA DIPHENYLPROLINOL TRIMETHYLSILYL ETHER; ALPHA,BETA UNSATURATED CARBONYL COMPUND; CARBONYL DERIVATIVE; CYCLOHEXANE DERIVATIVE; NITROSTYRENE; PENTANE 1,5 DIAL; TRIMETHYLSILYL DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; CALCULATION; CATALYSIS; CHEMICAL REACTION; CHEMICAL STRUCTURE; DIASTEREOISOMER; DIASTEREOSELECTIVITY; ENANTIOSELECTIVITY; PRIORITY JOURNAL; STEREOCHEMISTRY; SYNTHESIS;

EID: 82955203651     PISSN: 00404020     EISSN: 14645416     Source Type: Journal    
DOI: 10.1016/j.tet.2011.11.019     Document Type: Article

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